Laura Martí-Sánchez

3PUBLICATIONS
28CO-AUTHORS
Neurology and neuromuscular diseases
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Publications (3)

|Sep 22, 2026
A Novel KCNA1 Variant in a Patient With Tremor and Autism Spectrum Disorder Causes Mixed LOF/GOF Defects of Kv1.1 Channels.

|Sep 29, 2021
CPEB alteration and aberrant transcriptome-polyadenylation lead to a treatable SLC19A3 deficiency in Huntington's disease.

Sara Picó, Alberto Parras, María Santos-Galindo

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Frequent Collaborators

2 joint publications

Juan Darío Ortigoza-Escobar

2 joint publications

Loreto Martorell

1 joint publications

Sara Picó

1 joint publications

Alberto Parras